Xu Zicheng, Li Xiao, Qin Zhiqiang, Xue Jianxin, Wang Jingyuan, Liu Zhentao, Cai Hongzhou, Yu Bin, Xu Ting, Zou Qin
Department of Urologic Surgery, The Affiliated Cancer Hospital of Jiangsu Province of Nanjing Medical University, Nanjing - PR China.
Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing - PR China.
Int J Biol Markers. 2017 Jul 24;32(3):e297-e304. doi: 10.5301/ijbm.5000269.
Individual studies of the association between N-acetyltransferase 1 (NAT1)*10 allele and bladder cancer susceptibility have shown inconclusive results. To derive a more precise estimation of any such relationship, we performed this systemic review and updated meta-analysis based on 17 publications.
A total of 17 studies were investigated with 4,322 bladder cancer cases and 4,944 controls. The pooled odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the association. Subgroup analyses were conducted based on ethnicity, sex, source of controls and detecting methods. Then trial sequential analysis was performed to evaluate whether the evidence of the results was sufficient and reduce the risk of type I error.
There was no association between NAT1*10 allele and bladder cancer risk in a random-effects model (OR = 0.96, 95% CI, 0.84-1.10) or in a fixed-effects model (OR = 0.95, 95% CI, 0.87-1.03). In addition, no significantly increased risk of bladder cancer was found in any other subgroup analysis. Then, trial sequential analyses demonstrated that the results of our study need to be further verified.
Despite its limitations, the results of the present meta-analysis suggested that there was no association between NAT110 allele and bladder cancer risk. More importantly, our findings need to be further validated regarding whether being without the NAT110 allele could in the future be shown to be a potential marker for the risk of bladder cancer.
关于N - 乙酰基转移酶1(NAT1)*10等位基因与膀胱癌易感性之间关联的个别研究结果尚无定论。为了更精确地估计这种关系,我们基于17篇出版物进行了这项系统评价和更新的荟萃分析。
共调查了17项研究,其中包括4322例膀胱癌病例和4944例对照。采用合并比值比(OR)及95%置信区间(CI)来评估关联强度。基于种族、性别、对照来源和检测方法进行亚组分析。然后进行试验序贯分析,以评估结果的证据是否充分,并降低I型错误风险。
在随机效应模型(OR = 0.96,95%CI:0.84 - 1.10)或固定效应模型(OR = 0.95,95%CI:0.87 - 1.03)中,NAT1*10等位基因与膀胱癌风险之间均无关联。此外,在任何其他亚组分析中均未发现膀胱癌风险显著增加。然后,试验序贯分析表明我们研究的结果需要进一步验证。
尽管存在局限性,但本荟萃分析结果表明NAT110等位基因与膀胱癌风险之间无关联。更重要的是,关于未来是否能证明无NAT110等位基因是膀胱癌风险的潜在标志物,我们的研究结果需要进一步验证。